Xu Zhigao, Xu Peipei, Fan Wei, Yang Gui, Wang June, Cheng Qingyuan, Yu Mingxia
Department of Pathology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China.
Center for Gene Diagnosis, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China.
Exp Ther Med. 2017 Oct;14(4):3491-3500. doi: 10.3892/etm.2017.5003. Epub 2017 Aug 22.
Antitumor necrosis factor (TNF) agents have been widely used for the treatment of spondyloarthritis (SpA) and ankylosing spondylitis (AS). However, these agents may increase the risk of infection due to suppressing the immune response. The present meta-analysis was performed to systematically investigate the risk of overall infection, serious infection and tuberculosis in patients with SpA and AS treated with anti-TNF agents. Medline, Embase and the Cochrane library were searched for randomized controlled trials (RCTs) published between January 1998 and December 2015 about infection in patients with SpA receiving anti-TNF therapy. Data were pooled to obtain relative risks (RRs) along with their 95% confidence intervals (CIs). A total of 25 RCTs investigating SpA, including 12 investigating AS specifically, were eligible for the meta-analysis. Similar risks of overall infection were reported in patients with SpA (RR, 1.03; 95% CI, 0.92-1.15) and AS (RR, 1.06; 95% CI, 0.91-1.24) treated with anti-TNF agents. The RR of serious infection for patients with SpA or AS receiving anti-TNF therapy compared with a placebo was 1.27 (95% CI, 0.67-2.38) and 1.57 (95% CI, 0.63-3.91), respectively. In addition, 4 RCTs with outcomes of tuberculosis in patients with SpA receiving anti-TNF agents were identified, all in infliximab-treated patients (RR, 2.52; 95% CI, 0.53-12.09). However, due to the limited number of RCTs, this finding should be interpreted with caution. The present meta-analysis did not find any significantly increased risk of infection associated with anti-TNF therapy in patients with SpA or AS. However, due to short duration of follow-up in the RCTs and the rarity of serious infections and tuberculosis, patients treated with anti-TNF agents still should be closely monitored in clinical practice.
抗肿瘤坏死因子(TNF)药物已被广泛用于治疗脊柱关节炎(SpA)和强直性脊柱炎(AS)。然而,这些药物可能会因抑制免疫反应而增加感染风险。本荟萃分析旨在系统研究接受抗TNF药物治疗的SpA和AS患者发生总体感染、严重感染和结核病的风险。检索了Medline、Embase和Cochrane图书馆,以查找1998年1月至2015年12月期间发表的关于接受抗TNF治疗的SpA患者感染情况的随机对照试验(RCT)。汇总数据以获得相对风险(RR)及其95%置信区间(CI)。共有25项研究SpA的RCT符合荟萃分析的条件,其中12项专门研究AS。接受抗TNF药物治疗的SpA患者(RR,1.03;95%CI,0.92 - 1.15)和AS患者(RR,1.06;95%CI,0.91 - 1.24)报告的总体感染风险相似。与安慰剂相比,接受抗TNF治疗的SpA或AS患者发生严重感染的RR分别为1.27(95%CI,0.67 - 2.38)和1.57(95%CI,0.63 - 3.91)。此外,还确定了4项有接受抗TNF药物治疗的SpA患者结核病结局的RCT,均为接受英夫利昔单抗治疗的患者(RR,2.52;95%CI,0.53 - 12.09)。然而,由于RCT数量有限,这一发现应谨慎解读。本荟萃分析未发现抗TNF治疗与SpA或AS患者感染风险显著增加有关。然而,由于RCT的随访时间较短,且严重感染和结核病罕见,在临床实践中仍应对接受抗TNF药物治疗的患者进行密切监测。